Evidence map›Paper›PMID 10921948›Full record

ArticleJournal of clinical microbiology2000

Rapid detection and identification of Candida, Aspergillus, and Fusarium species in ocular samples using nested PCR.

E E Jaeger, N M Carroll, S Choudhury, A A Dunlop, H M Towler, M M Matheson, P Adamson, N Okhravi, S Lightman

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02850653 (Contribution of Fast Molecular Bacterial Identification by Real-time PCR in Managing of Postoperative Acute Endophthalmitis), which is not on this map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
11.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02850653 naunknown statusnot on this mapstarted 2007, after this paper: background citation

Contribution of Fast Molecular Bacterial Identification by Real-time PCR in Managing of Postoperative Acute Endophthalmitis

TypeinterventionalSponsorUniversity Hospital, GrenobleRan2007 to 2016Enrolled150ConditionsAcute Endophthalmitis Post-operativeArmsPCR : 16S ribosomal DNA and real-time targeted PCR, Sampling of aqueous humour
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 171 citations in OpenAlex.

  1. Aspergillus Polymerase Chain Reaction: Systematic Review of Evidence for Clinical Use in Comparison With Antigen Testing.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
    Pooled it
  2. Review
  3. Article
  4. First Report ofPathogens (Basel, Switzerland) · 2025
    Article
  5. Article
  6. An Evaluation of the OLMJournal of fungi (Basel, Switzerland) · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Endogenous endophthalmitis: diagnosis, management, and prognosis.Journal of ophthalmic inflammation and infection · 2015
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Novel diagnosis of fungal endophthalmitis by broad-range real-time PCR detection of fungal 28S ribosomal DNA.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2012
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

E E JaegerDepartment of Clinical Ophthalmology, The Institute of Ophthalmology and Moorfields Eye Hospital, London EC1V 9EL, United Kingdom.
N M Carroll
S Choudhury
A A Dunlop
H M Towler
M M Matheson
P Adamson
N Okhravi
S Lightman
Moorfields Eye Hospital NHS Foundation Trust · GBWhipps Cross University Hospital · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

A protocol for the rapid detection of fungal DNA in ocular samples, derived from three species, Candida albicans, Aspergillus fumigatus, and Fusarium solani, has been developed. Two novel panfungal primers complementary to 18S rRNA sequences present in all three species were designed. Panfungal PCR was followed by three nested PCRs utilizing species-specific primers. PCR sensitivity ranged from 50 to 100 fg of free DNA and between one and two C. albicans organisms. In addition, we also developed a rapid and reliable DNA extraction protocol. This protocol minimized DNA loss during extraction, whilst removing compounds from vitreous and aqueous fluids that have previously been shown to have inhibitory effects on PCR. Preliminary results obtained after testing the protocol on three patient samples support culture results and medical history. However, one patient was PCR positive but culture negative, suggesting that the sensitivity of this protocol may exceed that of traditional culture techniques. This system, therefore, constitutes an additional protocol that may significantly aid patient management in cases where fungal endophthalmitis is suspected.

Indexed as

AspergillosisAspergillus fumigatusCandida albicansCandidiasisDNA, FungalDNA PrimersEndophthalmitisEye Infections, FungalFusariumHumansPolymerase Chain ReactionSensitivity and SpecificitySpecies SpecificityVitrectomyVitreous BodyDNA, FungalDNA Primers

Identifiers

PMID10921948
PMCPMC87142
OpenAlexW2167146516

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.